Sparteine
98.0%
- Product Code: 69052
Alias:
Spartine
CAS:
492-08-0
| Molecular Weight: | 234.39 g./mol | Molecular Formula: | C₁₅H₂₆N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00869353 | |
| Melting Point: | 201℃ | Boiling Point: | |
| Density: | 1.08 | Storage Condition: | room temperature |
Product Description:
Sparteine is primarily used in organic chemistry as a chiral base or ligand in asymmetric synthesis, aiding in the creation of enantiomerically pure compounds. It is particularly valuable in the synthesis of pharmaceuticals, where the specific spatial arrangement of molecules can significantly impact drug efficacy and safety. Additionally, sparteine has been employed in the resolution of racemic mixtures, helping to separate enantiomers for further use in drug development. Historically, it was also used in medicine as an antiarrhythmic agent, though its clinical use has declined due to the availability of safer alternatives. In research, sparteine continues to be a useful tool for studying stereochemistry and reaction mechanisms.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 98 100% |
| REFRACTIVE INDEX N20D | 1.526-1.531 |
| SPECIFIC ROTATION A20DC1 ETOH | 16 19 |
| INFRARED SPECTROMETRY | Conforms to Structure |
| APPEARANCE | Colorless to yellow liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿990.00 |
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| 1.000 | 10-20 days | ฿2,920.00 |
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Sparteine
Sparteine is primarily used in organic chemistry as a chiral base or ligand in asymmetric synthesis, aiding in the creation of enantiomerically pure compounds. It is particularly valuable in the synthesis of pharmaceuticals, where the specific spatial arrangement of molecules can significantly impact drug efficacy and safety. Additionally, sparteine has been employed in the resolution of racemic mixtures, helping to separate enantiomers for further use in drug development. Historically, it was also used in medicine as an antiarrhythmic agent, though its clinical use has declined due to the availability of safer alternatives. In research, sparteine continues to be a useful tool for studying stereochemistry and reaction mechanisms.
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